Resorbable barrier micro-membranes for attenuation of scar tissue during healing

ABSTRACT

Resorbable polylactide polymer scar tissue reduction barrier membranes and methods of their application are disclosed. The scar-tissue reduction barrier membranes are constructed entirely of polylactide resorbable polymers, which are engineered to be absorbed into the body relatively slowly over time in order to reduce potential negative side effects. The scar tissue reduction barrier membranes are formed to have thicknesses on the order of microns, such as, for example, thicknesses between 10 and 300 microns. The membranes are preshaped with welding flanges and stored in sterile packaging.

RELATED APPLICATIONS

[0001] This application claims the benefit of priority under 35 U.S.C.section 119(e) of provisional application No. 60/231,800, filed Sep. 11,2000, and of provisional application No. 60/196,869, filed Mar. 10,2000.

FIELD OF THE INVENTION

[0002] The present invention relates generally to medical devices and,more particularly, to devices and methods for attenuating the formationof post-surgical adhesions between a post-surgical site and adjacentsurrounding tissue.

BACKGROUND OF THE INVENTION

[0003] A major clinical problem relating to surgical repair orinflammatory disease is adhesion which occurs during the initial phasesof the healing process after surgery or disease. Adhesion is a conditionwhich involves the formation of abnormal tissue linkages. These linkageswhich form can impair bodily function, produce infertility, obstruct theintestines and other portions of the gastrointestinal tract (bowelobstruction) and produce general discomfort, e.g. pelvic pain. Thecondition can be life threatening. The most common form of adhesionoccurs after surgery as a result of surgical interventions, althoughadhesion may occur as a result of other processes or events such aspelvic inflammatory disease, mechanical injury, radiation treatment andthe presence of foreign material.

[0004] Various attempts have been made to prevent postoperativeadhesions. For example, the use of peritoneal lavage, heparinizedsolutions, procoagulants, modification of surgical techniques such asthe use of microscopic or laparoscopic surgical techniques, theelimination of talc from surgical gloves, the use of smaller sutures andthe use of physical barriers (membranes, gels or solutions) aiming tominimize apposition of serosal surfaces, have all been attempted.Unfortunately, very limited success has been seen with these methods.Barrier materials, in various forms such as membranes and viscousintraperitoneal solutions, which are designed to limit tissueapposition, have also met with only limited success. The best of thesebarrier materials include cellulosic barriers, polytetrafluoroethylenematerials, and dextran solutions.

[0005] U.S. Pat. No. 5,795,584 to Tokahura et al. discloses ananti-adhesion or scar tissue reduction films or membranes, and U.S. Pat.No. 6,136,333 to Cohn, et al. discloses a similar structure. In theTokahura patent, a bioabsorbable polymer is copolymerized with asuitable carbonate and then formed into a non-porous single layeradhesion barrier, such as a film. In the Cohn patent, a polymerichydrogel for anti-adhesion is formed without crosslinking by usingurethane chemistry. Both of these patents involved relatively complexchemical formulas and/or reactions to result in a particular structureto be used as surgical adhesion barriers.

SUMMARY OF THE INVENTION

[0006] Resorbable polylactide polymer scar tissue reduction barriermembranes and methods of their application have been discovered. Inaccordance with one aspect of the present invention, the scar-tissuereduction barrier membranes are constructed entirely of polylactideresorbable polymers, which are engineered to be absorbed into the bodyrelatively slowly over time in order to reduce potential negative sideeffects. The scar tissue reduction barrier membranes are formed to havethicknesses on the order of microns, such as, for example, thicknessesbetween 10 and 300 microns. The membranes are preshaped with weldingflanges and stored in sterile packaging.

BRIEF DESCRIPTION OF THE DRAWINGS

[0007]FIG. 1 illustrates a laminotomy procedure wherein a portion of theposterior arch (lamina) of a vertebra is surgically removed;

[0008]FIG. 2 is an enlarged view of FIG. 2;

[0009]FIG. 3 illustrates a scar-reduction resorbable barriermicro-membrane for application to the exiting nerve root of the spinalchord in accordance with a first pre-formed embodiment of the presentinvention;

[0010]FIG. 4 illustrates a scar-reduction resorbable barriermicro-membrane for application to two exiting nerve roots of the spinalchord in accordance with a second pre-formed embodiment of the presentinvention;

[0011]FIG. 5 illustrates a scar-reduction resorbable barriermicro-membrane for application to four exiting nerve roots of the spinalchord in accordance with a third pre-formed embodiment of the presentinvention;

[0012]FIG. 6a is a top planar view of a scar-reduction resorbablebarrier membrane in accordance with a fourth pre-formed embodiment ofthe present invention;

[0013]FIG. 6b is a cross-sectional view of the scar-reduction resorbablebarrier membrane shown in FIG. 6a;

[0014]FIG. 7a is a top planar view of a scar-reduction resorbablebarrier membrane in accordance with a fifth pre-formed embodiment of thepresent invention;

[0015]FIG. 7b is a cross-sectional view of the scar-reduction resorbablebarrier membrane shown in FIG. 7a;

[0016]FIG. 8a is a top planar view of a scar-reduction resorbablebarrier membrane in accordance with a sixth pre-formed embodiment of thepresent invention;

[0017]FIG. 8b is a cross-sectional view of the scar-reduction resorbablebarrier membrane shown in FIG. 8a;

[0018]FIG. 9a is a top planar view of a scar-reduction resorbablebarrier membrane in accordance with a seventh pre-formed embodiment ofthe present invention;

[0019]FIG. 9b is a cross-sectional view of the scar-reduction resorbablebarrier membrane shown in FIG. 9a;

[0020]FIG. 10a is a top planar view of a scar-reduction resorbablebarrier membrane in accordance with an eighth pre-formed embodiment ofthe present invention;

[0021]FIG. 10b is a cross-sectional view of the scar-reductionresorbable barrier membrane shown in FIG. 10a;

[0022]FIG. 11a is a top planar view of a scar-reduction resorbablebarrier membrane in accordance with a ninth pre-formed embodiment of thepresent invention;

[0023]FIG. 11b is a cross-sectional view of the scar-reductionresorbable barrier membrane shown in FIG. 11a;

[0024]FIG. 12a is a top planar view of a scar-reduction resorbablebarrier membrane in accordance with a tenth pre-formed embodiment of thepresent invention;

[0025]FIG. 12b is a cross-sectional view of the scar-reductionresorbable barrier membrane shown in FIG. 12a;

[0026]FIG. 13a is a top planar view of a scar-reduction resorbablebarrier membrane in accordance with an eleventh pre-formed embodiment ofthe present invention;

[0027]FIG. 13b is a cross-sectional view of the scar-reductionresorbable barrier membrane shown in FIG. 13a;

[0028]FIG. 14a is a top planar view of a scar-reduction resorbablebarrier membrane in accordance with a twelfth pre-formed embodiment ofthe present invention;

[0029]FIG. 14b is a cross-sectional view of the scar-reductionresorbable barrier membrane shown in FIG. 14a;

[0030]FIG. 15a is a top planar view of a scar-reduction resorbablebarrier membrane in accordance with a thirteenth pre-formed embodimentof the present invention;

[0031]FIG. 15b is a cross-sectional view of the scar-reductionresorbable barrier membrane shown in FIG. 15a;

[0032]FIG. 16a is a top planar view of a scar-reduction resorbablebarrier membrane in accordance with a fourteenth pre-formed embodimentof the present invention;

[0033]FIG. 16b is a cross-sectional view of the scar-reductionresorbable barrier membrane shown in FIG. 16a;

[0034]FIG. 17a is a top planar view of a scar-reduction resorbablebarrier membrane in accordance with a fifteenth pre-formed embodiment ofthe present invention; and

[0035]FIG. 17b is a cross-sectional view of the scar-reductionresorbable barrier membrane shown in FIG. 17a.

[0036]FIG. 18 is illustrates a scar-reduction resorbable barriermicro-membrane of the present invention implanted on a rat spine, withtwo spinus processes of the spine protruding at opposing ends of theimplant;

[0037]FIG. 19 is a bar graph showing the results of a study comparingthe scar-reduction barrier membrane of the present invention againstseveral other materials, and controls, indicating the percent collagenfound in and around the dura following a surgical procedure after aperiod of about three weeks;

DETAILED DESCRIPTION OF THE PRESENTLY PREFERRED EMBODIMENTS

[0038] The present invention provides a resorbable implant in membraneform that can be used in various surgical contexts to retard or preventtissue adhesions, and reduce scarring. The polylactide polymers andco-polymers of the present invention require relatively simple chemicalreactions and formulations. It is believed that the presentscar-reduction resorbable barrier membranes of polylactide polymers andco-polymers can induce relatively minor localized tissue inflammation,but that inflammation is believed to be minimized as a result of thepresently engineered compositions, constructions, and applications asset forth herein, to thereby yield highly effective scar tissuereduction.

[0039] The scar-reduction resorbable barrier membrane of the presentinvention may be more effective than other membranes because it is verysmooth and non-porous. Moreover, the barrier membrane is preferablybioabsorbable in the body. The lack of porosity acts to form a barrierthat does not allow interaction of the tissues. The non-porosity and thesmoothness of the barrier membrane can reduce tissue turbulence, enhancetissue guidance, and minimize scar formation. Moreover, the smooth,uninterrupted surface of the barrier membrane material may facilitatemovement of the dura and local tissues across the area, hence reducingfrictional rubbing and wearing which may induce scar tissue formation.

[0040] As used herein, the term “non-porous” refers to a material whichis generally water tight and, in accordance with a preferred embodiment,not fluid permeable. However, in a modified embodiment of the inventionmicro-pores (i.e., fluid permeable but not cell permeable) may exist inthe scar-reduction resorbable barrier membrane of the present invention,to the extent, for example, that they do not substantially disrupt thesmoothness of the surfaces of the resorbable barrier membrane to causescarring of tissue. In substantially modified embodiments for limitedapplications, pores which are cell permeable but not vessel permeablemay be manufactured and used. As presently preferred, the resorbablebarrier membrane is manufactured using a press molding procedure toyield a substantially non-porous film. The barrier membrane materials ofpresent invention may have a semi-rigid construction, and are fullycontourable when heated to approximately 55 degrees Celsius. Aspresently embodied, many of the thinner membrane thicknesses can besufficiently contoured even in the absence of heating.

[0041] The material can be used in a number of surgical applications,including: surgical repair of fracture orbital floors, surgical repairof the nasal septum and perforated ear drum barrier membrane, as aprotective sheathing to facilitate osteogenesis, surgical repair of theurethral anatomy and repair of urethral strictures, prevention ofsynostosis in completed corrective surgery for cranial fusions andforearm fractures, lessening of soft-tissue fibrosis or bony growth, asa temporary covering for prenatal rupture omphalocele during stagedrepair procedures, guided tissue regeneration between the teeth andgingival margin, tympanic membrane repairs, dural coverings and neuralrepair, heart vessel repair, hernia repair, tendon anastomoses,temporary joint spacers, wound dressings, scar coverings, and as acovering for gastroschisis. The barrier membrane material of the presentinvention is particularly suitable for preventing tissue from abnormallyfibrotically joining together following surgery, which can lead toabnormal scarring and interfere with normal physiological functioning.In some cases, such scarring can force and/or interfere with follow-up,corrective, or other surgical operations. For example, there is evidencepointing to epidural adhesions as possible factors contributing tofailed back surgery. Epidural fibrosis may occur following spinalinjuries or as a post-operative surgical complication. The dense scarformation on dura and around nerve roots has previously been describedas the “laminotomy membrane,” and has been implicated in renderingsubsequent spine operations technically more difficult. In alamininectomy procedure, for example, the scar-reduction resorbablebarrier membrane of the present invention is desirably inserted betweenthe dural sleeve and the paravertebral musculature post laminotomy andconforms readily to block exposed marrow elements of the laminae.Imposition of the membrane material as a barrier between theparavertebral musculature and the epidural space is believed to reducecellular trafficking and vascular invasion into the epidural space fromthe overlying muscle and adjacent exposed cancellous bone. Moreover,tests have shown that the present barrier membrane material does notappear to interfere with normal posterior wound healing while at thesame time inhibiting the unwanted adhesions and scarring.

[0042] In a preferred embodiment of the present invention, the barriermembrane material comprises a poly lactide polymer or co-polymer and,more preferably, comprises 70:30 poly L-lactide-co-D and poly L-lactide(PLA). As presently embodied, the material comprises poly(L-lactide-co-D,L-lactide) 70:30 Resomer LR708 manufactured and suppliedfrom Boehringer Ingelheim KG of Germany. A pre-formed membrane made fromPLA can be shaped at the time of surgery by bringing the material to itsglass transition temperature, using heating iron, hot air, heated spongeor hot water bath methods. The scar-tissue reduction barrier membrane ofthe present invention preferably has a uniform thickness of less thanabout 300 microns, preferably less than 200 microns, and more preferablybetween 10 microns and 100 microns. As defined herein, the“micro-membranes” of the present invention comprise thicknesses between10 microns and 300 microns and, preferably, between 10 and 100 microns.

[0043] The very thin construction of these micro-membranes is believedto substantially accelerate the rate of absorption of the implants,compared to rates of absorption of thicker membrane implants of the samematerial. It is believed, however, that resorption into the body tooquickly of the micro-membrane will yield undesirable drops in local pHlevels, thus introducing/elevating, for example, local inflammation,discomfort and/or foreign antibody responses. Further, a resultinguneven (e.g., cracked, broken, roughened or flaked) surface of a barriermembrane degrading too early may undesirably cause tissue turbulencebetween the tissues before, for example, adequate healing has occurred,resulting in potential tissue inflammation and scarring. It is believedthat a micro-membrane of the present invention having a thickness ofabout 200 microns or less should maintain its structural integrity for aperiod in excess of three weeks and, more preferably for at least 7weeks, before substantially degrading, so that the anti-scarringfunction can be achieved and optimized. To the extent the micro-membranedoes not degrade at an accelerated rate, compared to a thicker membraneof the same material, the membrane should maintain its structuralintegrity for a period in excess of 6 months and, more preferably for atleast one year, before substantially degrading, in order to achieve andoptimize the anti-scarring function. The polylactide resorbable polymerbarrier membranes in accordance with this aspect of the presentinvention are thus designed to resorb into the body at a relatively slowrate.

[0044] The object of reducing acidity levels and/or tissue turbulence,and any accompanying inflammation (e.g., swelling), at the post-surgicalsite is believed to be of particular importance in the context of spinalsurgeries, which are often performed for the very purpose of relievinginflammation-induced discomfort. It is believed that nerve tissue can beparticularly sensitive to, for example, slightly elevated acidity levelsand inflammation. During a typical spinal surgical procedure, such as,for example, a laminotomy, a portion of the lamina structure is removedfrom a patient's vertebrae in order to, for example, provide access tothe spinal column and/or disk.

[0045] The barrier membrane material may be provided in rectangularmembranes that are for example several centimeters on each side, or canbe cut and formed into specific shapes, configurations and sizes by themanufacturer before packaging and sterilization. In modifiedembodiments, various known formulations and copolymers of poly lactidesmay affect the physical properties of the scar-reduction resorbablebarrier membrane and/or the bridging membrane. The thin barriermembranes of the present invention are sufficiently flexible to conformaround anatomical structures, although some heating in a hot water bathmay be necessary for thicker configurations. In modified embodiments,certain poly lactides which become somewhat more rigid and brittle atthicknesses above 0.25 mm and which can be softened by formation with acopolymer and another polylactide, for example, may be implemented toform scar-reduction resorbable barrier micro-membrane. Moreover, inaccordance with another aspect of the present invention, the scar-tissuereduction barrier micro-membrane and/or the bridging membrane, (definedinfra) may comprises a substance for cellular control, such as at leastone of a chemotactic substance for influencing cell-migration, aninhibitory substance for influencing cell-migration, a mitogenic growthfactor for influencing cell proliferation, a growth factor forinfluencing cell differentiation, and factors which promoteneoangiogenesis (formation of new blood vessels).

[0046] Referring more particularly to the drawings, FIG. 1 illustrates alaminotomy procedure wherein a the two vertebrae 20 and 22 are separatedand fixated using screws 24 and rods 26, and a portion of the lamina hasbeen removed, leaving a window 28 (shown as a phantom rectangle) in thevertebrae 22. FIG. 2 is an enlarged view of the window 28 in the laminaof the vertebrae 22. The spinal chord 30 and an exiting nerve root 32are thus exposed. In accordance with the present invention, thescar-reduction resorbable barrier micro-membrane is applied to the duraof both the spinal chord 30 and the exiting nerve root 32, to therebyattenuate or eliminate the occurrence of post-operative scarring in thevicinity of the exiting nerve root 32. In a modified embodiment, athicker bridging membrane is applied to one or both of the vertebrae 20and 22, to thereby bridge (i.e., tent) over and cover the window 28.This bridging membrane may be non-porous, fluid permeable, cellpermeable or vessel permeable in accordance with various embodiments,and preferably comprises a thickness between about 0.5 mm and 2.0 mm forpreventing prolapse of adjacent muscle tissue into the foramen (i.e.,the spinal lumen containing the spinal chord 30 and exiting nerve root32). In accordance with various embodiments, the bridging membrane maybe used alone or in combination with the scar-reduction resorbablebarrier micro-membrane or, the scar-reduction resorbable barriermembrane may be used without the bridging membrane.

[0047] Various means for attaching the barrier membrane to structuressuch as muscular tissue, other soft tissue, or bone are contemplated.For example, sutures or staples may be used to attach the membrane tothe paravertebral muscle. As another example, the bridging membrane inparticular may be secured to the vertebrae bone using resorbable bonescrews or tacks. Tucking or folding the membrane material intoanatomical crevices may be sufficient to fix its position. An adhesivesuch as a fibrin sealant, or a resorbable cyanoacrylate adhesive mayfurther be utilized to secure the membranes, alone or in combinationwith the above means of attachment.

[0048] In accordance with one aspect of the present invention, thescar-reduction resorbable barrier micro-membrane can be heat bonded,such as with a bipolar electro-cautery device, ultrasonicly welded, orsimilarly sealed directly to the dura of the spinal chord 30 and theexiting nerve root 32. Such a device can be used to heat the barriermembrane at various locations, such as at the edges and at points in themiddle, at least above its glass transition temperature, and preferablyabove its softening point temperature. The glass transition temperatureof the preferred material (70:30 poly L-lactide-co-D and poly L-lactide(PLLA)) is about 55° Celsius., while its softening point temperature isabove 110° Celsius. The material is heated along with adjacent tissuesuch that the two components bond together at their interface. Inanother embodiment, the scar-reduction resorbable barrier membrane canbe heat bonded or sealed directly to one or both of the vertebrae 20 and22, or to muscle or other soft tissue, for example. In yet anotherembodiment, the scar-reduction resorbable barrier micro-membrane can beheat bonded or sealed directly to itself in an application, for example,wherein the micro-membrane is wrapped around a structure and then heatjoined to itself. Moreover, the technique of heat-sealing the barriermembrane material to itself or body tissue may be combined with anotherattachment method for enhanced anchoring. For example, the barriermembrane material may be temporarily affixed in position using two ormore points of heat sealing (i.e., heat welding) using anelectro-cautery device, and sutures, staples or glue can then be addedto secure the barrier membrane into place.

[0049] Turning to FIG. 3, a pre-formed scar-reduction resorbable barriermicro-membrane 34 is formed with a first welding flange 36 and a secondwelding flange 38 thereon. A trunk portion 40 fits over the spinal chord30, and a branch portion 42 fits over the exiting nerve root 32. Thefirst welding flange 36 is formed by a first slit 44 and a second slit46, and the second welding flange 38 is formed by a first slit 48 and asecond slit 50. In application, the pre-formed scar-reduction resorbablebarrier micro-membrane 34 is placed over the spinal chord 30 and theexiting nerve root 32 and, subsequently, the first welding flange 36 andthe second welding flange 38 are bent at least partially around theexiting nerve root. The rounded end 52 of the branch portion 42 fitsonto a portion of the exiting nerve root 32 furthest away from thespinal chord 30. As presently embodied, the first welding flange 36 andthe second welding flange are wrapped around, and preferably tuckedbeneath (i.e., behind) the exiting nerve root 32. In a preferredembodiment, the first welding flange 36 is then heat welded to thesecond welding flange 38. The flanges preferably are cut to wrapentirely around the exiting nerve root 32 and overlap one another. Thefirst welding flange 36 may be sutured to the second welding flange 38,alone or in addition with the heat welding step, to thereby secure thefirst welding flange 36 to the second welding flange 38. In anotherembodiment, neither heat welding nor suturing are used and the flangesare merely tucked partially or completely around the exiting nerve root32 (depending on the dimensions of the root 32). When sutures are to beused, the pre-formed scar-reduction resorbable barrier micro-membrane 34may be pre-formed and packaged with optional suture apertures 60. Theedges 64 and 66 are then preferably heat welded to the spinal chord 30.The two edges 68 and 70 form a third welding flange 72. A fourth weldingflange 74 is formed by slits 76 and 78, and a fifth welding flange 80 isformed by slits 82 and 84. The welding flanges may be secured in mannerssimilar to those discussed in connection with the welding flanges 36 and38. Heat welds may further be secured along other edges and along thesurface of the pre-formed scar-reduction resorbable barriermicro-membrane 34, such as shown at 90 in FIG. 18. Moreover, notches maybe formed on the membranes of the present invention, such as, forexample, at the ends 64 and 66 in modified-shape embodiments, foraccommodating, for example, the spinal processes. Such exemplary notchesare shown in FIG. 18 and 92.

[0050]FIG. 4 illustrates a scar-reduction resorbable barriermicro-membrane for application to two exiting nerve roots 32 and 98 ofthe spinal chord in accordance with another pre-formed embodiment of thepresent invention. FIG. 5 illustrates a scar-reduction resorbablebarrier micro-membrane similar to that of FIG. 4 but adapted forapplication to four exiting nerve roots of the spinal chord inaccordance with another pre-formed embodiment of the present invention.For example, the branch portion 100 is analogous in structure andoperation to the branch portion 42 of the FIG. 3 embodiment, and theother branch portion 102 is constructed to accommodate the exiting nerveroot 98. Simlar elements are shown in FIG. 5 at 100 a, 102 a, 100 b and102 c. The embodiments of FIGS. 6-17 illustrate other configurations foraccommodating different anatomical structures. For example, theconfigurations of FIGS. 7, 10, 12, 14 and 15 are designed to be formedinto, for example, a cone structure to fit around a base portion with aprotrusion extending through the center of the membrane. The illustratedembodiments of FIGS. 6-17 have suture perforations formed around theirperimeters, and many are shown with cell and vessel permeable pores.

[0051] In accordance with the present invention, the pre-formedscar-reduction resorbable barrier micro-membranes are preformed andsealed in sterilized packages for subsequent use by the surgeon. Sincean objective of the scar-reduction resorbable barrier micro-membranes ofthe present invention is to reduce sharp edges and surfaces,preformation of the membranes is believed to help facilitate, albeit toa relatively small degree, rounding of the edges for less rubbing,tissue turbulence and inflammation. That is, the surfaces and any sharpedges of the scar-reduction resorbable barrier micro-membranes arebelieved to be capable of slightly degrading over time in response toexposure of the membranes to moisture in the air, to thereby formrounder edges. This is believed to be an extremely minor effect.Moreover, sterilization processes (E-beam or heat) on the cut,pre-packaged and/or packaged membrane can further round any sharp edges,as can any initial heating to glass temperature of the pre-cut membranesjust before implanting. Moreover, the very thin scar-reductionresorbable barrier micro-membranes of the present invention may beparticularly susceptible to these phenomena, and, perhaps to a morenoticeable extent, are susceptible to tearing or damage from handling,thus rendering the pre-forming of the scar-reduction resorbable barriermicro-membranes beneficial for preserving the integrity thereof.

[0052] An embodiment of the scar-reduction resorbable barrier membranehas been tested in rat studies in comparison with several scar-tissuereduction barrier gels with favorable results. Specifically, the barriermembrane material of the present invention and the scar-tissue reductiongels were inserted around the spinal column of 52 male adultSprague-Dawley rats, each weighing 400 plus grams. A posterior midlineincision was made exposing the bony posterior elements from L4 to L7,and bilateral laminectomies were performed at the L5 and L6 level usingsurgical loupes. Following the laminectomies, the dura was retractedmedially (to the left then to the right) using a microscope to exposethe disc at L5/L6, and a bilateral controlled disc injury was performedusing a 26 gauge needle. After hemostasis and irrigation, ananti-inflammatory agent was applied over both laminectomy sites.

[0053] The rats were divided and treated in five groups: 1) normalcontrols without surgery; 2) untreated, laminectomy only; 3) those towhich 0.1 cc of high molecular weight hyaleronan (HA gel) was applied tothe laminectomy site; 4) those to which 0.1 cc of Adcon-L scar-tissuereduction gel was applied to the laminectomy site; and 5) those that hadan insertion of a barrier membrane of the present invention over thelaminectomy site. The wounds were closed in a routine manner, and thesurvival period was three weeks.

[0054] After termination of each of the rats, the L5 segmental nerveroots were dissected free bilaterally using an anterior approach. Thesegmental nerve roots were excised including the portion of the nerveroot within the foramen (1 cm in length). Additionally, the dura wasexposed using an anterior approach. The dura from the caudal aspect ofthe body of L4 to the cephalad aspect of the body of L7 was removed (1.5center in length) including all attached scar. The samples were analyzedbiochemical by extracting the fat, then vacuum drying and determiningthe amount of total collagen and the percent of collagen from thehydroxyproline content. The amount of total collagen was expressed inmilligrams and the percent of collagen was expressed as a percent of fatfree dry weight.

[0055] Each treatment group was compared to both the normal controls andthe operated but untreated controls using a Fisher's multiplecomparisons paired t-test. Additionally, the treatment groups werecompared using a one-way analysis of variance. In the untreated,laminotomy-only specimens, the total collagen increased more thantwo-fold in the dura (p value of 0.0009). In the untreated group, thepercent collagen increased significantly in both the dura and nerveroots (p values of 0.001 and 0.005, respectively). Treatment with HA gel(p=0.010), Adcon-L (p=0.004), or the barrier membrane of the presentinvention (p=0.002) significantly reduced the amount of total collagenin the dura. Likewise, the same holds true for the percent collagenwhere the values are: HA gel (p=0.015), Adcon-L (p=0.041), and thebarrier membrane of the present invention (p=0.011). There was a trendshowing that the barrier membrane of the present invention decreasedapproximately 50% more both in total collagen and percent collagencompared to the HA gel and Adcon-L. In the nerve roots, the amount oftotal collagen and a percentage of collagen was not significantlychanged by treatment with any of the HA gel, Adcon-L, or barriermembrane of the present invention.

[0056] These biochemical measurements of total and percent collagenenabled obtension of quantitative data on scar formation postlaminotomy. Gross findings and biochemical analysis in the modeldemonstrated that the untreated laminotomy scar becomes adherent to thedorsum of the dura mater, a clearly undesirable outcome. Both a singleapplication of HA gel or Adcon-L demonstrated a beneficial effect at thelevel of the dura. However, the half life of HA gel is less than 24hours, and the Adcon-L is resorbed within approximately four weeks,which suggests that further long-term studies could be conducted.Additionally, Adcon-L has the potential to delay posterior woundhealing, possibly leading to wound infections and/or wound dehiscences(few of the adverse events experienced by less than 1% of the studygroups per product pamphlet). On the other hand, the barrier membrane ofthe present invention appears to wall off the overlying muscle,potentially protecting against cellular trafficking and vascularingrowth, and does not appear to interfere with normal posterior woundhealing. A possible improvement on the results obtained by using thebarrier membrane of the present invention by itself may be obtained byusing the barrier membrane in conjunction with an anti-inflammatory gelagent applied, for example, beneath the barrier membrane. Additionally,the scar-tissue reduction barrier membrane may be used in combinationwith a fixation device for stabilizing the bone defect, such as shown inconnection with the two vertebrae 20 and 22 of FIG. 1.

[0057]FIG. 19 illustrates a bar graph showing the percent collagenresulting from the aforementioned rat tests for various groups. Theresults for the barrier membrane of the present invention are labeled asMacropore, while the last result denoted MAC+HA is for the membranematerial of the present mention in conjunction with HA gel. The resultsindicate that there is a marked improvement over the HA gel or Adcon-L,and significant improvement in comparison with a tissue growth factorbeta and a material known as Decorin.

[0058] While the foregoing is a complete description of the preferredembodiments of the invention, various alternatives, modifications, andequivalents may be used. Moreover, it will be obvious that certain othermodifications may be practiced within the scope of the appended claims.

What is claimed is:
 1. A resorbable scar-tissue reduction micro-membranefor attenuating a formation of post-surgical scar tissue between ahealing post-surgical site and adjacent surrounding tissue following anin vivo surgical procedure on the post-surgical site, the implant havinga pre-implant configuration, which is defined as a configuration of theimplant immediately before the implant is formed between thepost-surgical site and the adjacent surrounding tissue, the implantcomprising. a substantially planar membrane of resorbable polymer basematerial having a first substantially-smooth side and a secondsubstantially-smooth side, the substantially planar membrane ofresorbable polymer base material comprising a single layer of resorbablepolymer base material between the first substantially-smooth side andthe second substantially-smooth side, the single layer of resorbablepolymer base material having a substantially uniform composition;wherein a thickness of the single layer of resorbable polymer basematerial, measured between the first substantially-smooth side and thesecond substantially-smooth side, is between about 10 microns and about300 microns; wherein the single layer of resorbable polymer basematerial is non-porous; and wherein the single layer of resorbablepolymer base material consists essentially of a material selected fromthe group consisting of: a poly-lactide polymer; and a copolymer of twoor more poly-lactides; and wherein the single layer of resorbablepolymer base material is adapted to maintain a smooth-surfaced barrierbetween the healing post-surgical site and the adjacent surroundingtissue for a relatively extended period of time sufficient to attenuateor eliminate any formation of scar tissue between the post-surgical siteand the adjacent surrounding tissue, and is adapted to be resorbed intothe mammalian body within a period of approximately 18 to 24 months froman initial implantation of the implant into the mammalian body.
 2. Theresorbable scar-tissue reduction micro-membrane as set forth in claim 1,wherein the resorbable polymer base material is 70:30 poly(L-lactide-co-D,L-lactide) (PLA).
 3. The resorbable scar-tissuereduction micro-membrane as set forth in claim 1, wherein the resorbablepolymer base material is poly-L-lactide (PLLA).
 4. The resorbablescar-tissue reduction micro-membrane set forth in claim 1, wherein thethickness is about 100 microns.
 5. The resorbable scar-tissue reductionmicro-membrane as set forth in claim 1, wherein the thickness is about200 microns.
 6. The resorbable scar-tissue reduction micro-membrane asset forth in claim 1, wherein the single layer of resorbable polymerbase material is not fluid permeable.
 7. The resorbable scar-tissuereduction micro-membrane as set forth in claim 1, wherein the resorbablescar-tissue reduction micro-membrane is impregnated with at least one ofa chemotactic substance for influencing cell-migration, an inhibitorysubstance for influencing cell-migration, a mitogenic growth factor forinfluencing cell proliferation, a growth factor for influencing celldifferentiation, and factors which promote neoangiogenesis (formation ofnew blood vessels).
 8. The resorbable scar-tissue reductionmicro-membrane set forth in claim 1, wherein the resorbable scar-tissuereduction micro-membrane is sealed in a sterile packaging.
 9. Theresorbable scar-tissue reduction micro-membrane set forth in claim 8,wherein the resorbable scar-tissue reduction micro-membrane comprises aplurality of holes disposed along an edge of the resorbable scar-tissuereduction micro-membrane.
 10. The resorbable scar-tissue reductionmicro-membrane set forth in claim 9, wherein the edge extends around theresorbable scar-tissue reduction micro-membrane.
 11. The resorbablescar-tissue reduction micro-membrane set forth in claim 10, wherein theresorbable scar-tissue reduction micro-membrane does not comprise anyholes substantially away from the edge of the resorbable scar-tissuereduction micro-membrane.
 12. The resorbable scar-tissue reductionmicro-membrane set forth in claim 11, wherein a slit is formed in aperiphery of the resorbable scar-tissue reduction micro-membrane so thatthe edge extends along the slit.
 13. The resorbable scar-tissuereduction micro-membrane set forth in claim 10, wherein: the resorbablescar-tissue reduction micro-membrane further comprises a plurality ofholes disposed away from the edge; each of the holes near the peripheryhas a first diameter; each of the holes near the center has a seconddiameter; and the first diameters are greater than the second diameters.14. The resorbable scar-tissue reduction micro-membrane set forth inclaim 13, wherein a slit is formed in a periphery of the resorbablescar-tissue reduction micro-membrane so that the edge extends along theslit.
 15. The resorbable scar-tissue reduction micro-membrane set forthin claim 8, wherein the resorbable scar-tissue reduction micro-membranecomprises a slit disposed in the non-porous base material.
 16. Theresorbable scar-tissue reduction micro-membrane set forth in claim 8,wherein the resorbable scar-tissue reduction micro-membrane is cut tohave a size and shape suitable for snugly and anatomically fitting overthe dura of an exiting nerve root to thereby attenuate formation of scartissue between the dura and surrounding muscular tissue, and is sealedin a sterile packaging.
 17. The resorbable scar-tissue reductionmicro-membrane set forth in claim 8, wherein the resorbable scar-tissuereduction micro-membrane is cut with tabs to be folded over and aroundan anatomic.
 18. The resorbable scar-tissue reduction micro-membrane setforth in claim 8, wherein the resorbable scar-tissue reductionmicro-membrane comprises a notch disposed in the non-porous basematerial.
 19. The resorbable scar-tissue reduction micro-membrane setforth in claim 8, wherein the resorbable scar-tissue reductionmicro-membrane comprises a plurality of notches disposed in thenon-porous base material.
 20. The resorbable scar-tissue reductionmicro-membrane set forth in claim 1, wherein the resorbable scar-tissuereduction micro-membrane is cut to have a non-rectangular andnon-circular shape and is sealed in a sterile packaging.
 21. Theresorbable scar-tissue reduction micro-membrane set forth in claim 2,wherein the resorbable scar-tissue reduction micro-membrane is cut tohave a size and shape suitable for snugly and anatomically fitting overthe dura of an exiting nerve root to thereby attenuate formation of scartissue between the dura and surrounding muscular tissue, and is sealedin a sterile packaging.
 22. The resorbable scar-tissue reductionmicro-membrane set forth in claim 2, wherein the resorbable scar-tissuereduction micro-membrane is cut with tabs to be folded over and aroundan anatomic structure and is sealed in a sterile packaging.
 23. Theresorbable scar-tissue reduction micro-membrane set forth in claim 2,wherein the thickness is about 100 microns.
 24. The resorbablescar-tissue reduction micro-membrane as set forth in claim 2, whereinthe thickness is about 200 microns.
 25. The resorbable scar-tissuereduction micro-membrane as set forth in claim 2, wherein the singlelayer of resorbable polymer base material is not fluid permeable. 26.The resorbable scar-tissue reduction micro-membrane as set forth inclaim 1, wherein the resorbable scar-tissue reduction micro-membrane isimpregnated with at least one of a chemotactic substance for influencingcell-migration, an inhibitory substance for influencing cell-migration,a mitogenic growth factor for influencing cell proliferation, a growthfactor for influencing cell differentiation, and factors which promoteneoangiogenesis (formation of new blood vessels).
 27. The resorbablescar-tissue reduction micro-membrane set forth in claim 2, wherein theresorbable scar-tissue reduction micro-membrane is sealed in a sterilepackaging.
 28. A resorbable scar-tissue reduction membrane forattenuating a formation of post-surgical scar tissue between a healingpost-surgical site and adjacent surrounding tissue following an in vivosurgical procedure on the post-surgical site, the implant having apre-implant configuration, which is defined as a configuration of theimplant immediately before the implant is formed between thepost-surgical site and the adjacent surrounding tissue, the implantcomprising: a substantially planar membrane of resorbable polymer basematerial having a first substantially-smooth side and a secondsubstantially-smooth side, the substantially planar membrane ofresorbable polymer base material comprising a layer of resorbablepolymer base material between the first substantially-smooth side andthe second substantially-smooth side, the layer of resorbable polymerbase material having a substantially uniform composition; wherein athickness of the layer of resorbable polymer base material, measuredbetween the first substantially-smooth side and the secondsubstantially-smooth side, is between about 10 microns and about 300microns; wherein the layer of resorbable polymer base material isnon-porous; and wherein the layer of resorbable polymer base materialconsists essentially of a material selected from the group consistingof: a poly-lactide; and a copolymer of two or more poly-lactides; andwherein the substantially planar membrane of resorbable polymer basematerial is sealed in a sterile packaging and is pre-formed to be cut tobe formed around an sterile.
 29. The resorbable scar-tissue reductionmicro-membrane set forth in claim 28, wherein the resorbable scar-tissuereduction micro-membrane is cut to have a non-rectangular andnon-circular shape, is cut to anatomically fit over and protect anexiting nerve root, and is sealed in a sterile packaging.
 30. Theresorbable scar-tissue reduction micro-membrane set forth in claim 28,wherein the resorbable scar-tissue reduction micro-membrane is cut tohave a non-rectangular and non-circular shape, is cut with tabs to befolded over and around and to protect an exiting nerve root, and issealed in a sterile packaging.
 31. The resorbable scar-tissue reductionmicro-membrane set forth in claim 28, wherein the resorbable scar-tissuereduction micro-membrane is cut to have a non-rectangular andnon-circular shape and is sealed in a sterile packaging.
 32. Theresorbable scar-tissue reduction micro-membrane set forth in claim 28,wherein the resorbable scar-tissue reduction micro-membrane is cut tohave a non-rectangular and non-circular shape, is cut to anatomically.33.
 33. The resorbable scar-tissue reduction micro-membrane set forth inclaim 28, wherein the membrane comprises a substantially planar membraneof resorbable polymer base material having a first substantially-smoothside and the second substantially-smooth side, the substantially planarmembrane of resorbable polymer base material comprising a single layerof resorbable polymer base material between the firstsubstantially-smooth side and the second substantially-smooth side, thesingle layer of resorbable polymer base material having a substantiallyuniform composition.